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Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia

Authors :
Jordi Pérez-Tur
C. Lo Nigro
Theologia Sarafidou
Panagiotis Deloukas
Roberto Michelucci
Marco Seri
Rosanna Zimbello
André Rosenthal
Carlo Nobile
Paolo Scannapieco
Reiner Siebert
J. J. Poza
Carlo Alberto Tassinari
S Gesk
Lisa French
Brigitte Schlegelberger
Bernd Hinzmann
Nicholas K. Moschonas
A. López de Munain
Alfredo Ciccodicola
Giorgio Valle
Source :
Gene (Amst.) 282 (2002): 87–94. doi:10.1016/S0378-1119(01)00846-0, info:cnr-pdr/source/autori:Nobile C, Hinzmann B, Scannapieco P, Siebert R, Zimbello R, Perez-Tur J, Sarafidou T, Moschonas NK, French L, Deloukas P, Ciccodicola A, Gesk S, Poza JJ, Lo Nigro C, Seri M, Schlegelberger B, Rosenthal A, Valle G, Lopez de Munain A, Tassinari CA, Michelucci R./titolo:Identification and characterization of a novel human brain-specific gene, homologous to S. Scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia./doi:10.1016%2FS0378-1119(01)00846-0/rivista:Gene (Amst.)/anno:2002/pagina_da:87/pagina_a:94/intervallo_pagine:87–94/volume:282
Publication Year :
2002

Abstract

We describe the structure, genomic organization, and some transcription features of a human brain-specific gene previously localized to the genomic region involved in temporal lobe epilepsy and spastic paraplegia on chromosome 10q24. The gene, which consists of six exons disseminated over 16 kb of genomic DNA, is highly homologous to the porcine tmp83.5 gene and encodes a putative transmembrane protein of 141 amino acids. Unlike its porcine homolog, from which two mRNAs with different 5'-sequences are transcribed, the human gene apparently encodes three mRNA species with 3'-untranslated regions of different sizes. Mutation analysis of its coding sequence in families affected with temporal lobe epilepsy or spastic paraplegia linked to 10q24 do not support the involvement of this gene in either diseases. (C) 2002 Elsevier Science B.V. All rights reserved.

Details

ISSN :
03781119
Volume :
282
Issue :
1-2
Database :
OpenAIRE
Journal :
Gene
Accession number :
edsair.doi.dedup.....bc36ef0ca65eee4d82d0632ff46454e7
Full Text :
https://doi.org/10.1016/S0378-1119(01)00846-0